4-(2-Aminophenyl)benzyl alcohol

Base Information

Chemical Name:4-(2-Aminophenyl)benzyl alcohol
CAS No.:873056-45-2
Molecular Formula:C₁₃H₁₃NO
Molecular Weight:199.252
Hs Code.:
DSSTox Substance ID:DTXSID20362738
Wikidata:Q82146103
Mol file:873056-45-2.mol

Synonyms:873056-45-2;4-(2-AMINOPHENYL)BENZYL ALCOHOL;(2'-Amino-[1,1'-biphenyl]-4-yl)methanol;SCHEMBL393770;DTXSID20362738;SB85225

Suppliers and Price of 4-(2-Aminophenyl)benzyl alcohol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
(2'-Amino-[1,1'-biphenyl]-4-yl)methanol 97%
1g
$ 370.00

American Custom Chemicals Corporation
4-(2-AMINOPHENYL)BENZYL ALCOHOL 95.00%
5MG
$ 495.65

Total 1 raw suppliers

Chemical Property of 4-(2-Aminophenyl)benzyl alcohol

Chemical Property:

PSA：46.25000
LogP:3.00930
XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:199.099714038
Heavy Atom Count:15
Complexity:187

Purity/Quality:: (2'-Amino-[1,1'-biphenyl]-4-yl)methanol 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C2=CC=C(C=C2)CO)N

Technology Process of 4-(2-Aminophenyl)benzyl alcohol

There total 3 articles about 4-(2-Aminophenyl)benzyl alcohol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 5737-79-1
methyl 2′-amino-[1,1′-biphenyl]-4-carboxylate

: 873056-45-2
2-amino-4'-hydroxymethylbiphenyl

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at -10 - 20 ℃; for 24h;
DOI:10.1002/ejoc.201601043

Reference yield:

: 99768-12-4
4-methoxycarbonylphenylboronic acid

: 873056-45-2
2-amino-4'-hydroxymethylbiphenyl

Guidance literature:: Multi-step reaction with 2 steps

1: sodium carbonate; palladium diacetate / ethylene glycol; water / 24 h / 80 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / 24 h / -10 - 20 °C

With lithium aluminium tetrahydride; palladium diacetate; sodium carbonate; In tetrahydrofuran; water; ethylene glycol; 1: |Suzuki Coupling;
DOI:10.1002/ejoc.201601043

Reference yield:

: 615-36-1
2-bromoaniline

: 873056-45-2
2-amino-4'-hydroxymethylbiphenyl

Guidance literature:: Multi-step reaction with 2 steps

1: sodium carbonate; palladium diacetate / ethylene glycol; water / 24 h / 80 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / 24 h / -10 - 20 °C

With lithium aluminium tetrahydride; palladium diacetate; sodium carbonate; In tetrahydrofuran; water; ethylene glycol; 1: |Suzuki Coupling;
DOI:10.1002/ejoc.201601043